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α-Nitro-stilbene is an organic compound characterized by its molecular formula C14H11NO2, which consists of a stilbene core with a nitro group attached to the alpha carbon. Stilbene itself is a derivative of benzene with two phenyl rings connected by an ethene bridge. The α-nitro group in α-nitro-stilbene is positioned at the carbon atom adjacent to the double bond, which influences the compound's reactivity and properties. This yellow crystalline solid is sensitive to light and heat, and it is used in the synthesis of various dyes and pharmaceuticals. Due to its reactive nature, α-nitro-stilbene can undergo a range of chemical reactions, such as reduction and rearrangement, making it a valuable intermediate in organic chemistry.

82864-83-3

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82864-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82864-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,6 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82864-83:
(7*8)+(6*2)+(5*8)+(4*6)+(3*4)+(2*8)+(1*3)=163
163 % 10 = 3
So 82864-83-3 is a valid CAS Registry Number.

82864-83-3Relevant academic research and scientific papers

Aerobic carbon-carbon bond cleavage of alkenes to aldehydes catalyzed by first-row transition-metal-substituted polyoxometalates in the presence of nitrogen dioxide

Rubinstein, Amir,Jiménez-Lozanao, Pablo,Carbó, Jorge J.,Poblet, Josep M.,Neumann, Ronny

, p. 10941 - 10948 (2014)

A new aerobic carbon-carbon bond cleavage reaction of linear di-substituted alkenes, to yield the corresponding aldehydes/ketones in high selectivity under mild reaction conditions, is described using copper(II)-substituted polyoxometalates, such as {α2-Cu(L)P2W 17O61}8- or {[(Cu(L)]2WZn(ZnW 9O34)2}12-, as catalysts, where L = NO2. A biorenewable-based substrate, methyl oleate, gave methyl 8-formyloctanoate and nonanal in >90% yield. Interestingly, cylcoalkenes yield the corresponding epoxides as products. These catalysts either can be prepared by pretreatment of the aqua-coordinated polyoxometalates (L = H 2O) with NO2 or are formed in situ when the reactions are carried with nitroalkanes (for example, nitroethane) as solvents or cosolvents. Nitroethane was shown to release NO2 under reaction conditions. 31P NMR shows that the Cu-NO2-substituted polyoxometalates act as oxygen donors to the C-C double bond, yielding a Cu-NO product that is reoxidized to Cu-NO2 under reaction conditions to complete a catalytic cycle. Stoichiometric reactions and kinetic measurements using {α2-Co(NO2)P2W17O 61}8- as oxidant and trans-stilbene derivatives as substrates point toward a reaction mechanism for C-C bond cleavage involving two molecules of {α2-Co(NO2)P2W 17O61}8- and one molecule of trans-stilbene that is sufficiently stable at room temperature to be observed by 31P NMR.

Synthesis of Benzo[4,5]imidazo[2,1-b]thiazole by Copper(II)-Catalyzed Thioamination of Nitroalkene with 1H-Benzo[d]imidazole-2-thiol

Jana, Sourav,Chakraborty, Amrita,Shirinian, Valerii Z.,Hajra, Alakananda

supporting information, p. 2402 - 2408 (2018/05/08)

A Copper(II)-catalyzed thioamination of β-nitroalkene with 1H-benzo[d]imidazole-2-thiol has been developed for the synthesis of benzo[4,5]imidazo[2,1-b]thiazole derivatives. A variety of N-fused benzoimidazothiazole derivatives are obtained in high yields through successive C?N and C?S bond formations. This protocol is also applicable to β-substituted β-nitroalkenes to afford 2,3-disubstituted benzoimidazothiazoles. (Figure presented.).

Iron(III) nitrate-induced aerobic and catalytic oxidative cleavage of olefins

Amaya, Toru,Fujimoto, Hayato

supporting information, p. 2657 - 2660 (2018/06/04)

Microwave-assisted catalytic oxidative cleavage of olefins using Fe(NO3)3·9H2O under O2 is reported. This reaction system is particularly effective when 9-benzylidene-9H-fluorene derivatives are used as substrates even though they are tri- and tetra-substituted olefins.

PREPARATION OF ALDEHYDES AND KETONES FROM ALKENES USING POLYOXOMETALATE CATALYSTS AND NITROGEN OXIDES

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Paragraph 0115, (2017/03/21)

The present invention relates to a process for preparing aldehydes and ketones by carbon-carbon bond cleavage of alkenes, wherein the process is catalysed by first row transition metal nitro coordinated polyoxometalate catalyst. The catalyst can be prepared by pre-treatment of aqua coordinated polyoxometalates with NO2, or they are formed in situ when the reactions are carried in nitroalkanes under aerobic conditions, or they are formed in situ from nitrosyl (NO) compounds in the presence of O2.

Iron-catalyzed tandem one-pot addition and cyclization of the blaise reaction intermediate and nitroolefins: Synthesis of substituted NH-pyrroles from nitriles

Zhao, Mi-Na,Liang, Hao,Ren, Zhi-Hui,Guan, Zheng-Hui

supporting information, p. 221 - 226 (2013/03/13)

The iron-catalyzed addition and cyclization of the Blaise reaction intermediate and nitroolefins to synthesize highly functionalized NH-pyrroles in a tandem one-pot manner from nitriles has been developed. This reaction shows good functional group tolerance and affords a broad spectrum of substituted NH-pyrroles in good yields. Copyright

Acetyl chloride - Silver nitrate - Acetonitrile: A reagent system for the synthesis of 2-nitroglycals and 2-nitro-1-acetamido sugars from glycals

Kancharla, Pavan K.,Reddy, Y. Suman,Dharuman, Suresh,Vankar, Yashwant D.

experimental part, p. 5832 - 5837 (2011/09/20)

A new reagent system comprising acetyl chloride, silver nitrate, and acetonitrile has been developed for the synthesis of 2-nitroglycals from the corresponding glycals. Under certain conditions, the formation of 2-nitro-1-acetamido sugars has also been observed. In addition, a few other non-carbohydrate-derived olefins also gave the corrresponding conjugated nitroolefins.

The Reaction of Phenylethylenes with NO2

Bryant, Duncan K.,Challis, Brian C.,Iley, Jim

, p. 1027 - 1028 (2007/10/02)

Nitrogen dioxide reacts with phenylethylenes to yield several products that can be explained by radical addition of two NO2 molecules; the relevance of these reactions to the formation of nitropolycyclic aromatic hydrocarbons in the environment is discussed.

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